Forecasted Shifts in Thermal Habitat for Cod Species in the Northwest Atlantic and Eastern Canadian Arctic

Climate change will alter ecosystems and impose hardships on marine resource users as fish assemblages redistribute to habitats that meet their physiological requirements. Marine gadids represent some of the most ecologically and socio-economically important species in the North Atlantic, but face an uncertain future in the wake of rising ocean temperatures. We applied CMIP5 ocean temperature projections to egg survival and juvenile growth models of three northwest Atlantic coastal species of gadids (Atlantic cod, Polar cod, and Greenland cod), each with different thermal affinities and life histories. We illustrate how physiologically based species distribution models (SDMs) can be used to predict habitat distribution shifts and compare vulnerabilities of species and life stages with changing ocean conditions. We also derived an integrated habitat suitability index from the combined surfaces of each metric to predict areas and periods where thermal conditions were suitable for both life stages. Suitable thermal habitat shifted poleward for the juvenile life stages of all three species, but the area remaining differed across species and life stages through time. Arctic specialists like Polar cod are predicted to experience reductions in suitable juvenile habitat based on metrics of egg survival and growth potential. In contrast, habitat loss in boreal and subarctic species like Atlantic cod and Greenland cod may be dampened due to increases in suitable egg survival habitats as suitable juvenile growth potential habitats decrease. These results emphasize the need for mechanistic SDMs that can account for the combined effects of changing seasonal thermal requirements under varying climate change scenarios.

Selected life history traits of Leptaxis simia (Gastropoda: Hygromiidae) established in the laboratory

Among ten adult specimens of the Madeiran endemic land snail Leptaxis simia kept in the laboratory, a single clutch of 110 eggs was reared, and the mortality, growth and reproductive capacity of hatchlings over a 1240- day period were monitored. Of 70 hatchlings, 34 survived to complete shell growth at around 640 days. Growth was rapid, and mortality high in the early stages; growth slowed and mortality was very low as full size was approached. Snails kept singly failed to lay any eggs. Among those with potential mates, only three clutches were produced, one of which yielded no hatchlings. Clutches were produced at least five months after shell growth was complete. Mortality increased sharply after the onset of sexual maturity, and the oldest snail survived for three and a half years. The apparently very strictly semelparous mode of reproduction, delayed sexual maturity and relatively long period of juvenile growth are discussed in relation to other species, and to the practical problems of rearing potentially endangered species in captivity.

Transgenerational effects decrease larval resilience to ocean acidification and warming but juvenile European sea bass could benefit from higher temperatures in the NE Atlantic

The aim of this study was to investigate the effect of ocean acidification (OA) and warming (OW) as well as the transgenerational effect of OA on larval and juvenile growth and metabolism of a large economically important fish species with a long generation time. Therefore we incubated European sea bass from Brittany (France) for two generations (>5 years in total) under current and predicted OA conditions (PCO2: 650 and 1700 μatm). In the F1 generation both OA condition were crossed with OW (temperature: 15-18 °C and 20-23 °C). We found that OA alone did not affect larval or juvenile growth and OW increased developmental time and growth rates, but OAW decreased larval size at metamorphosis. Larval routine metabolic rate (RMR) and juvenile standard metabolic rate (SMR) were significantly lower in cold compared to warm conditioned fish and also lower in F0 compared to F1 fish. We did not find any effect of OA on RMR or SMR. Juvenile PO2crit was not affected by OA, OW or OAW in both generations. We discuss the potential underlying mechanisms resulting in beneficial effects of OW on F1 larval growth and RMR and in resilience of F0 and F1 larvae and juveniles to OA, but on the other hand resulting in vulnerability of F1, but not F0 larvae to OAW. With regard to the ecological perspective, we conclude that recruitment of larvae and early juveniles to nursery areas might decrease under OAW conditions but individuals reaching juvenile phase might benefit from increased performance at higher temperatures.

Reproductive Allocation and Maternal Investment in Intertidal Whelks

<p>Parental investment per offspring is a key life history trait in which offspring size and number combinations are balanced in order to maximise fitness. When food is scarce and energy for reproduction is reduced, changes in reproductive allocation can be expected. These adjustments may go on to influence the growth and survival of the next generation. Trade-offs in reproductive allocation in response to food availability occurred differently in each of the three whelks species of this study. However, each species traded numbers of offspring rather than size of offspring when fed low food. Offspring size was more variable among and within capsules than among food treatments. Capsule size was a plastic trait that varied in response to food treatments in each of the species and varied among populations of the same species. Carry-over effects of maternal nutrition influenced juvenile growth in all three species. However, while juvenile growth was greater when adults were fed high food in two of the species, high adult food suppressed the growth of juveniles of the third species. This may be a mechanism to prevent potential negative consequences of rapid growth. There was no evidence of a maternal effect of mortality in any of the three species. Greater variation in hatchling size occurred in the species in which nurse egg feeding occurred. Nurse egg feeding may be a successful strategy in unpredictable environments where optimal offspring size changes from year to year. Regional differences in reproductive allocation between whelks separated by small distances suggest that populations may be isolated from one another and may need to be managed separately for conservation purposes. This study highlights the influence of maternal nutritional effects on life history and the potential impacts that these may have on population and community structure.</p>

Reproductive Allocation and Maternal Investment in Intertidal Whelks

<p>Parental investment per offspring is a key life history trait in which offspring size and number combinations are balanced in order to maximise fitness. When food is scarce and energy for reproduction is reduced, changes in reproductive allocation can be expected. These adjustments may go on to influence the growth and survival of the next generation. Trade-offs in reproductive allocation in response to food availability occurred differently in each of the three whelks species of this study. However, each species traded numbers of offspring rather than size of offspring when fed low food. Offspring size was more variable among and within capsules than among food treatments. Capsule size was a plastic trait that varied in response to food treatments in each of the species and varied among populations of the same species. Carry-over effects of maternal nutrition influenced juvenile growth in all three species. However, while juvenile growth was greater when adults were fed high food in two of the species, high adult food suppressed the growth of juveniles of the third species. This may be a mechanism to prevent potential negative consequences of rapid growth. There was no evidence of a maternal effect of mortality in any of the three species. Greater variation in hatchling size occurred in the species in which nurse egg feeding occurred. Nurse egg feeding may be a successful strategy in unpredictable environments where optimal offspring size changes from year to year. Regional differences in reproductive allocation between whelks separated by small distances suggest that populations may be isolated from one another and may need to be managed separately for conservation purposes. This study highlights the influence of maternal nutritional effects on life history and the potential impacts that these may have on population and community structure.</p>

Environmental and Life-history Factors Influencing Juvenile Demography of a Temperate Reef Fish

<p>Realistic population models and effective conservation strategies require a thorough understanding of the processes that drive variation in individual growth and survival, particularly within life stages that are subject to high mortality. For fragmented marine populations it is also important to consider how processes driving variation performance may vary through space and time. In this study I assess the interaction of two primary factors driving juvenile demography: benthic habitat composition and larval history traits, in a temperate reef fish, Forsterygion lapillum (the common triplefin). It is well understood that juveniles of many marine organisms are closely associated with structured nearshore habitats as they provide resources (refuge and food sources) that are critical for juvenile growth and/or survival. Nursery habitats are often assessed using measures of fitness of juveniles inhabiting them (e.g. rates of growth). However individual fitness measures may not only be indicative of conditions experienced in the benthic phase, but also an individual's prior history. Recent evidence suggests that variation in larval traits at settlement (e.g., size and age at settlement, larval growth rate) can impact on subsequent ecological performance (e.g., feeding ability and/or predator avoidance) and therefore influence subsequent fitness (i.e. rates of growth and/or probabilities of survival). I used otolith microstructure to assess separate and joint effects of habitat composition and larval traits on the growth of young F. lapillum. Both macroalgal composition of habitat patches and larval traits affected juvenile growth rates, and results suggested that habitat composition may have the potential to mediate fitness-related advantages that may accrue to certain individuals as a result of paternal effects and/or larval dispersal history. Quantifying spatio-temporal variability in the post-settlement fitness of Individuals with that differ in larval traits is essential for effective spatial management of marine populations. I further explore the joint effects of macroalgal composition and larval traits, within the context of additional spatial and temporal environmental variation. Results provide direct evidence that habitat can mediate the strength of carryover effects, but that the impact of habitat was variable between local populations and settlement events through time. In chapter 4 of my thesis, I focus on how small-scale variation in macroalgal composition within a nursery habitat (while controlling for individual variation) can affect the strength of density dependent growth and survival rates of F. lapillum. Density-dependent survival is evident during the first 30 days after settlement, and the strength of density dependence varied as a function of macroalgal composition. Resulting variation in estimates of nursery value (i.e., the number of late-stage juveniles produced per area unit of habitat) highlight the importance of incorporating local scale variation in juvenile demography into assessments of nursery habitat. Lastly, I assess a potential strategy of fishes to persist in a wide range of benthic environments. The ability to adjust traits (i.e., phenotypic plasticity) may allow organisms that encounter a range of unpredictable environmental conditions to maximise fitness within a single generation. In chapter 5 I explore patterns of variation in morphology of juvenile F. lapillum from two different subpopulations and from different macroalgal habitats. I evaluate possible evidence for constraints on morphological variation arising from variation in growth rate prior to and following settlement. Results suggest that for organisms with complex life cycles, variation in growth rates experienced during dispersal may constrain plasticity in later stages.</p>

Environmental and Life-history Factors Influencing Juvenile Demography of a Temperate Reef Fish

<p>Realistic population models and effective conservation strategies require a thorough understanding of the processes that drive variation in individual growth and survival, particularly within life stages that are subject to high mortality. For fragmented marine populations it is also important to consider how processes driving variation performance may vary through space and time. In this study I assess the interaction of two primary factors driving juvenile demography: benthic habitat composition and larval history traits, in a temperate reef fish, Forsterygion lapillum (the common triplefin). It is well understood that juveniles of many marine organisms are closely associated with structured nearshore habitats as they provide resources (refuge and food sources) that are critical for juvenile growth and/or survival. Nursery habitats are often assessed using measures of fitness of juveniles inhabiting them (e.g. rates of growth). However individual fitness measures may not only be indicative of conditions experienced in the benthic phase, but also an individual's prior history. Recent evidence suggests that variation in larval traits at settlement (e.g., size and age at settlement, larval growth rate) can impact on subsequent ecological performance (e.g., feeding ability and/or predator avoidance) and therefore influence subsequent fitness (i.e. rates of growth and/or probabilities of survival). I used otolith microstructure to assess separate and joint effects of habitat composition and larval traits on the growth of young F. lapillum. Both macroalgal composition of habitat patches and larval traits affected juvenile growth rates, and results suggested that habitat composition may have the potential to mediate fitness-related advantages that may accrue to certain individuals as a result of paternal effects and/or larval dispersal history. Quantifying spatio-temporal variability in the post-settlement fitness of Individuals with that differ in larval traits is essential for effective spatial management of marine populations. I further explore the joint effects of macroalgal composition and larval traits, within the context of additional spatial and temporal environmental variation. Results provide direct evidence that habitat can mediate the strength of carryover effects, but that the impact of habitat was variable between local populations and settlement events through time. In chapter 4 of my thesis, I focus on how small-scale variation in macroalgal composition within a nursery habitat (while controlling for individual variation) can affect the strength of density dependent growth and survival rates of F. lapillum. Density-dependent survival is evident during the first 30 days after settlement, and the strength of density dependence varied as a function of macroalgal composition. Resulting variation in estimates of nursery value (i.e., the number of late-stage juveniles produced per area unit of habitat) highlight the importance of incorporating local scale variation in juvenile demography into assessments of nursery habitat. Lastly, I assess a potential strategy of fishes to persist in a wide range of benthic environments. The ability to adjust traits (i.e., phenotypic plasticity) may allow organisms that encounter a range of unpredictable environmental conditions to maximise fitness within a single generation. In chapter 5 I explore patterns of variation in morphology of juvenile F. lapillum from two different subpopulations and from different macroalgal habitats. I evaluate possible evidence for constraints on morphological variation arising from variation in growth rate prior to and following settlement. Results suggest that for organisms with complex life cycles, variation in growth rates experienced during dispersal may constrain plasticity in later stages.</p>